comstat image-processing software Search Results


99
Oxford Instruments 6 3 1 software
6 3 1 Software, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
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MathWorks Inc comstat image-processing software
Comstat Image Processing Software, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
comstat image-processing software - by Bioz Stars, 2026-03
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MathWorks Inc image processing toolbox
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Average 90 stars, based on 1 article reviews
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96
MathWorks Inc matlab 5 1
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Average 96 stars, based on 1 article reviews
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MathWorks Inc matlab 5.1
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Carl Zeiss zen blue (2011) edition software
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Average 90 stars, based on 1 article reviews
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Nikon nis-elements ar software
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Nikon 3d images
Photodynamic eradication of C. albicans biofilms with TBTCP‐QY. A) Scheme for determining the changes in morphology and survival rates of mature C. albicans biofilms treated with or without TBTCP‐QY and light irradiation (80 mW cm −2 ) for 15 min. B) Representative <t>3D</t> <t>images</t> of C. albicans biofilms. Thirty‐six‐hour‐old mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX in the dark or irradiated with white light for 15 min (80 mW cm −2 ), followed by staining with a Live & Dead Viability/Cytotoxicity assay kit. A 488 nm laser and a 515–550 nm emission filter were employed for the green channel, and a 561 nm laser and a 570–620 nm emission filter were used for the red channel (scale bar: 50 µm). C) Representative FESEM images of C. albicans biofilms with different treatments. Mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX and then kept in the dark or irradiated with white light for 15 min (80 mW cm −2 ). The red arrows indicate deformed or destroyed fungal and hyphal cell envelopes (scale bar: 20 µm and 10 µm).
3d Images, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Evident Corporation fv10-asw 1.6
Photodynamic eradication of C. albicans biofilms with TBTCP‐QY. A) Scheme for determining the changes in morphology and survival rates of mature C. albicans biofilms treated with or without TBTCP‐QY and light irradiation (80 mW cm −2 ) for 15 min. B) Representative <t>3D</t> <t>images</t> of C. albicans biofilms. Thirty‐six‐hour‐old mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX in the dark or irradiated with white light for 15 min (80 mW cm −2 ), followed by staining with a Live & Dead Viability/Cytotoxicity assay kit. A 488 nm laser and a 515–550 nm emission filter were employed for the green channel, and a 561 nm laser and a 570–620 nm emission filter were used for the red channel (scale bar: 50 µm). C) Representative FESEM images of C. albicans biofilms with different treatments. Mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX and then kept in the dark or irradiated with white light for 15 min (80 mW cm −2 ). The red arrows indicate deformed or destroyed fungal and hyphal cell envelopes (scale bar: 20 µm and 10 µm).
Fv10 Asw 1.6, supplied by Evident Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Photodynamic eradication of C. albicans biofilms with TBTCP‐QY. A) Scheme for determining the changes in morphology and survival rates of mature C. albicans biofilms treated with or without TBTCP‐QY and light irradiation (80 mW cm −2 ) for 15 min. B) Representative 3D images of C. albicans biofilms. Thirty‐six‐hour‐old mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX in the dark or irradiated with white light for 15 min (80 mW cm −2 ), followed by staining with a Live & Dead Viability/Cytotoxicity assay kit. A 488 nm laser and a 515–550 nm emission filter were employed for the green channel, and a 561 nm laser and a 570–620 nm emission filter were used for the red channel (scale bar: 50 µm). C) Representative FESEM images of C. albicans biofilms with different treatments. Mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX and then kept in the dark or irradiated with white light for 15 min (80 mW cm −2 ). The red arrows indicate deformed or destroyed fungal and hyphal cell envelopes (scale bar: 20 µm and 10 µm).

Journal: Advanced Science

Article Title: A Membrane‐Targeted Photosensitizer Prevents Drug Resistance and Induces Immune Response in Treating Candidiasis

doi: 10.1002/advs.202207736

Figure Lengend Snippet: Photodynamic eradication of C. albicans biofilms with TBTCP‐QY. A) Scheme for determining the changes in morphology and survival rates of mature C. albicans biofilms treated with or without TBTCP‐QY and light irradiation (80 mW cm −2 ) for 15 min. B) Representative 3D images of C. albicans biofilms. Thirty‐six‐hour‐old mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX in the dark or irradiated with white light for 15 min (80 mW cm −2 ), followed by staining with a Live & Dead Viability/Cytotoxicity assay kit. A 488 nm laser and a 515–550 nm emission filter were employed for the green channel, and a 561 nm laser and a 570–620 nm emission filter were used for the red channel (scale bar: 50 µm). C) Representative FESEM images of C. albicans biofilms with different treatments. Mature biofilms were cocultured with 5 µ m TBTCP‐QY or 0.12% CHX and then kept in the dark or irradiated with white light for 15 min (80 mW cm −2 ). The red arrows indicate deformed or destroyed fungal and hyphal cell envelopes (scale bar: 20 µm and 10 µm).

Article Snippet: The 3D images were processed using NIS‐Elements AR software (Nikon) and Comstat2.

Techniques: Irradiation, Staining, Cytotoxicity Assay